Canonical Allele Identifier: PA2829689170
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 866389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Cys729Tyr
CA1396269
NM_007123.6:c.2186G>A